Possible Involvement of Smad Signaling Pathways in Induction of Odontoblastic Properties in KN-3 Cells by Bone Morphogenetic Protein-2: A Growth Factor to Induce Dentin Regeneration
Author(s) -
Ayako Washio,
Chiaki Kitamura,
Takahiko Morotomi,
Masamichi Terashita,
Tatsuji Nishihara
Publication year - 2012
Publication title -
international journal of dentistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.61
H-Index - 33
eISSN - 1687-8736
pISSN - 1687-8728
DOI - 10.1155/2012/258469
Subject(s) - odontoblast , microbiology and biotechnology , smad , dmp1 , bone morphogenetic protein 2 , bone morphogenetic protein , chemistry , signal transduction , alkaline phosphatase , dentinogenesis , bone morphogenetic protein 7 , bone morphogenetic protein 10 , phosphorylation , bone sialoprotein , intracellular , cell signaling , dentin , biology , biochemistry , pathology , osteocalcin , gene , in vitro , medicine , viral matrix protein , enzyme
We examined the effects of bone morphogenetic protein-2 (BMP-2) on growth, differentiation, and intracellular signaling pathways of odontoblast-like cells, KN-3 cells, to clarify molecular mechanisms of odontoblast differentiation during pulp regeneration process. After treatment with BMP-2, the cell morphology, growth, alkaline phosphatase (ALP) activity, and the activation and expression of BMP-induced intracellular signaling molecules, such as Smad1/5/8 and Smad6/7, as well as activities of dentin sialoprotein (DSP) and dentin matrix protein 1 (DMP1), were examined. BMP-2 had no effects on the morphology, growth, or ALP activity of KN-3 cells, whereas it induced the phosphorylation of Smad1/5/8 and expression of Smad6/7. BMP-2 also induced the expressions of DSP and DMP-1. Our results suggest that KN-3 cells may express an odontoblastic phenotype with the addition of BMP-2 through the activation of Smad signaling pathways.
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